Cargando…

Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome

We previously presented the protein-protein interaction network - the ‘HoP’ or the host protein interactome - of 332 host proteins that were identified to interact with 27 nCoV19 viral proteins by Gordon et al. Here, we studied drugs targeting the proteins in this interactome to identify whether any...

Descripción completa

Detalles Bibliográficos
Autores principales: Karunakaran, Kalyani B., Balakrishnan, N., Ganapathiraju, Madhavi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336709/
https://www.ncbi.nlm.nih.gov/pubmed/32702734
http://dx.doi.org/10.21203/rs.3.rs-30363/v1
_version_ 1783554372808998912
author Karunakaran, Kalyani B.
Balakrishnan, N.
Ganapathiraju, Madhavi
author_facet Karunakaran, Kalyani B.
Balakrishnan, N.
Ganapathiraju, Madhavi
author_sort Karunakaran, Kalyani B.
collection PubMed
description We previously presented the protein-protein interaction network - the ‘HoP’ or the host protein interactome - of 332 host proteins that were identified to interact with 27 nCoV19 viral proteins by Gordon et al. Here, we studied drugs targeting the proteins in this interactome to identify whether any of them may potentially be repurposable against SARS-CoV-2. We studied each of the drugs using the BaseSpace Correlation Engine and identified those that induce gene expression profiles negatively correlated with SARS-associated expression profile. This analysis resulted in 20 drugs whose differential gene expression (drug versus normal) had an anti-correlation with differential expression for SARS (viral infection versus normal). These included drugs that were already being tested for their clinical activity against SARS-CoV-2, those with proven activity against SARS-CoV/MERS-CoV, broad-spectrum antiviral drugs, and those identified/prioritized by other computational re-purposing studies. In summary, our integrated computational analysis of the HoP interactome in conjunction with drug-induced transcriptomic data resulted in drugs that may be repurposable for COVID-19.
format Online
Article
Text
id pubmed-7336709
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Journal Experts
record_format MEDLINE/PubMed
spelling pubmed-73367092020-07-14 Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome Karunakaran, Kalyani B. Balakrishnan, N. Ganapathiraju, Madhavi Res Sq Article We previously presented the protein-protein interaction network - the ‘HoP’ or the host protein interactome - of 332 host proteins that were identified to interact with 27 nCoV19 viral proteins by Gordon et al. Here, we studied drugs targeting the proteins in this interactome to identify whether any of them may potentially be repurposable against SARS-CoV-2. We studied each of the drugs using the BaseSpace Correlation Engine and identified those that induce gene expression profiles negatively correlated with SARS-associated expression profile. This analysis resulted in 20 drugs whose differential gene expression (drug versus normal) had an anti-correlation with differential expression for SARS (viral infection versus normal). These included drugs that were already being tested for their clinical activity against SARS-CoV-2, those with proven activity against SARS-CoV/MERS-CoV, broad-spectrum antiviral drugs, and those identified/prioritized by other computational re-purposing studies. In summary, our integrated computational analysis of the HoP interactome in conjunction with drug-induced transcriptomic data resulted in drugs that may be repurposable for COVID-19. American Journal Experts 2020-05-28 /pmc/articles/PMC7336709/ /pubmed/32702734 http://dx.doi.org/10.21203/rs.3.rs-30363/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Karunakaran, Kalyani B.
Balakrishnan, N.
Ganapathiraju, Madhavi
Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome
title Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome
title_full Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome
title_fullStr Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome
title_full_unstemmed Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome
title_short Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome
title_sort potentially repurposable drugs for covid-19 identified from sars-cov-2 host protein interactome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336709/
https://www.ncbi.nlm.nih.gov/pubmed/32702734
http://dx.doi.org/10.21203/rs.3.rs-30363/v1
work_keys_str_mv AT karunakarankalyanib potentiallyrepurposabledrugsforcovid19identifiedfromsarscov2hostproteininteractome
AT balakrishnann potentiallyrepurposabledrugsforcovid19identifiedfromsarscov2hostproteininteractome
AT ganapathirajumadhavi potentiallyrepurposabledrugsforcovid19identifiedfromsarscov2hostproteininteractome